Aromatic Cyclolinear Phosphazene Polyimides Based on a Novel Bis

Aug 1, 1995 - Carlos Díaz , Maria Luisa Valenzuela , Daniel Bravo , Vladimir Lavayen and Colm O'Dwyer. Inorganic Chemistry 2008 47 (24), 11561-11569...
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Macromolecules 1995,28,6323-6329

6323

Aromatic Cyclolinear Phosphazene Polyimides Based on a Novel Bis-Spiro-Substituted Cyclotriphosphazene Diamine Devendra Kumar*.+and Aka D. Guptat Polymeric Materials Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India Received February 15, 1995; Revised Manuscript Received June 5, 1995@

ABSTRACT: A new class of aromatic cyclolinear phosphazene polyimides has been synthesized from a novel bisspiro(ary1enedioxy)cyclotriphosphazenediamine.The geminal diamine, 2,2-bis(4'-aminophenoxy)4,4,6,6-bis[spiro(2',2"-dioxy-1',l"-biphenylyl)lcyclotriphosphazene (5) was polymerized by two-stage condensation polymerization with 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTDA, 7) and 4,4'hexafluoroisopropylidenediphthalic anhydride (GFDA, B), respectively. The obtained poly(amic acid)s 9 and 10 were spread on soda-lime glass plates with a doctor blade and left in a low-humidity chamber. The tack-free film of poly(amic acid) 9 was cyclodehydrated to a light-yellow polyimide (11)film by heating 1 h each at 100, 200, and 300 "C in a nitrogen atmosphere. The poly(amic acid) 10 on thermal cyclodehydration at 160 "C for 0.5 h, 235 "C for 1.5 h, and 280 "C for 0.5 h gave almost a colorless polyimide (12)film. The polyimide films showed good thermal stability and are noteworthy for their high char yield in air, viz., 58-50% at 800 "C. A simple and useful procedure was developed for the synthesis of polymer-grade monomer diamine (5). This involved substitution of 2,2-dichloro-4,4,6,6-bis[spiro(2',2"dioxy-l',l"-biphenylyl)]cyclotriphosphazene (3)with a potassium salt of 4-nitrophenol followed by catalytic 1"-biphenyly1)lcyclotriphreduction of the formed 2,2-bis(4'-nitrophenoxy)-4,4,6,6-bis[spiro(~,a"-dioxy-1', osphazene (4). The acetylation of diamine (5) gave 2,2-bis(4'-acetamidophenoxy)-4,4,6,6-bis[spiro(2',2"dioxy-1', 1"-biphenylyl)]cyclotriphosphazene (6)in 95% yield. The structures of these cyclic phosphazene precursors and monomer diamine were confirmed by J?T IR, 'H-NMR, 31P-NMRand differential scanning calorimetry (DSC).

Introduction Aromatic polyimides have found wide usage as films, coatings, adhesives, and matrix resins due t o their excellent electrical and mechanical properties, high thermal and chemical stability, good solvent resistance, and dimensional stability. For this reason they have been used in the aerospace, electronics industries,1s2a,b and membrane technologies2c for a wide variety of applications. The common strategies to obtain such materials involve incorporation of flexibilizing andor bulky groups into the polymer backbone. Cyclomatrix phosphazene polymers containing cyclotriphosphazene rings are known3 for their excellent fire resistance. These polymers are different from the well-known linear poly(pho~phazenes).~ In recent years, our group and others have developed exciting alternative methodologies for incorporating cyclotriphosphazenes into the structure of polymers. This approach is based on exploiting the reactivity of organofunctional cyclophosphazenes. We have successfully developed cyclotriphosphazene-containing poly( b i s m a l e i m i d e ~ ) , ~polyimides,8 ,~-~ poly(ether imide^),^ epoxy,1° and ethynyl typell matrix resins. The particular enhanced properties obtained were high char yield of polymers in air and nitrogen and 100%limited oxygen index (LOI) of their graphite cloth laminates. These polymers were developed from suitably end-capped hexakis(4-aminophenoxy)cyclotriphosphazene,tetrakis(4aminophenoxy)diphenoxycyclotriphosphazene, and tris(4-aminophenoxy)triphenoxycyclotriphosphazenes. It has been recognized that polyimide films such as Kapton-H degrade rapidly in low Earth orbit environ-

* Author to whom correspondence should be addressed. +Presentaddress: NASA Ames Research Center, MS: 239-14, Moffett Field, CA 94035-1000. Abstract published in Advance ACS Abstracts, August 1, 1995. @

ment by atomic oxygen12 and on exposure to oxygen plasma in a plasma reactor. It has been shown that a thin film coating of about 1000 of SiO, (where 1.9 5 x I 2.0) ion beam sputter deposited on Kapton-H can provide an adequate oxidation barrier. Such coatings, however, need special handling, and the coated polymeric material on exposure to atomic oxygen can be drastically eroded by an undercutting process at the defect sites. Hence, there is a definite need t o develop intrinsically stable improved polyimide films. For these and other reasons we have designed and synthesized a new cyclotriphosphazene-containingdiamine ( 5 ) to develop polyimide films with inherent fire- and heatresistance characteristics and stability toward oxygen atoms and oxygen plasmas. The 2,!2'-dioxybiphenylyl substitution was selected as it is possible13 t o synthesize mono- and bis-spirosubstituted cyclotriphosphazenes. Also, unlike several alkylenedioxy- and arylenedioxy-substitutedspirocyclot r i p h o ~ p h a z e n e s , ~tris(2,2'-dioxybiphenylyl)cyclotri~ phosphazene15 forms no inclusion adducts when recrystallized or brought into contact with organic solvents; furthermore, it is stable at least up to 350 "C and does not polymerize by ring-opening thermal polymerization. The structure of the selected bis-spiro substitution was expected to provide an opportunity of improved thermal stability and reduced flexibility of the dioxybiphenylyl spiro seven-membered ring. The diamine 5 was specially designed for this work and has several advantages: (1) The polymer-grade diamine can be conveniently synthesized in pure form and in high yield. (2) The selection of bis-spiro substitution on a cyclotriphosphazene ring was designed to exclude regioisomers, otherwise possible, and to synthesize a difunctional product with geminal orientation. In this paper, we describe the synthesis and characterization of novel hitherto unreported bis(ary1enediox-

0 1995 American Chemical Society 0024-9297/95/2228-6323$09.00~Q

6324 Kumar and Gupta

Macromolecules, Vol. 28, No. 18, 1995

continuous purge of nitrogen until no more water was collected in a Dean-Stark trap. The product obtained after removal of xylene was poured over crushed ice. The solid obtained was filtered, suspended in a 10% aqueous solution of potassium Experimental Section hydroxide, and washed successively with water. Drying in air Materials. Hexachlorocyclotriphosphazene (1) obtained and a vacuum desiccator provided a white solid (37 g, 90% from Nippon Soda Co., Ltd., Tokyo, Japan, was purified by yield). It was recrystallized from hot xylene to give shining sublimation a t 80-82 “C (0.1 mm), followed by recrystallizacrystals of 4,mp 263-264 “C. DSC: sharp endotherm at 266 tion from n-heptane. Differential scanning calorimetery (DSC) “C. Anal. Calcd for C ~ ~ H ~ ~ N ~C, P 55.4; ~ O I H, O 3.1; : N, 9.0; P, of purified trimer showed, as expected, a single sharp endo11.9%. Found: C, 55.6; H, 3.1; N, 9.1; P, 11.9. IR(KBrpellet, therm at 112.8 “C, while the mass spectrum indicated the cm-I): v 1519,1339 (asymmetrical and symmetrical stretching appropriate mass (m/z = 348). 4-Nitrophenol (Aldrich) was of the nitro group); 1613, 1582, 1482 (aromatic); 1200, 1179, purified by recrystallization from ethanol and dried in a 1115 (P-N-P asymmetrical stretching of cyclotriphosvacuum oven; mp 113- 115 “C. Potassium 4-nitrophenoxide phazene); 786 (P-N-P symmetrical stretching of cyclotriwas prepared by adding a solution of 4-nitrophenol in absolute phosphazene); 950 (P-N stretching of cyclotriphosphazene); ethanol into a solution of potassium hydroxide in absolute 1272 (ether). ‘H-NMR (DMSO-&): 6 7.27-7.29 (d, 4H aroethanol. The orange solid of potassium 4-nitrophenoxide was J = 7.4 matic, meta to nitro groups {=P(-O-C&-NOz)z}, dried in a vacuum oven; mp > 300 “C. Platinum oxide (Alpha Hz), 8.44-8.47 (d, 4H aromatic, ortho to nitro groups {EP(Product, 40 mesh) was used as received. N,N-DimethylacetaO-C,&-N02)2}, J = 7.4 Hz), 7.43-7.55 (m, 8H, aromatic mide (DMAC; Aldrich) was distilled over calcium hydride. protons of dioxybiphenylgroups), 7.60-7.61 and 7.64-7.65 (dd, Tetrabutylammonium bromide (TBAB) was used as received 4H, aromatic protons of dioxybiphenyl groups, J = 7.4 and 1.5 from Aldrich. Chlorobenzene (Aldrich) was distilled over Hz), 7.66-7.67 and 7.69-7.70 (dd, 4H, aromatic protons of anhydrous calcium chloride and stored on molecular sieves. dioxybiphenyl groups, J = 7.4 and 1.5 Hz). 2,2’-Dihydroxy-l,l’-biphenyl (Aldrich; 2)was used as received, 2,2-Bis(4-aminophenoxy)-4,4,6,6-bis[ spiro(2’,a”-dioxymp 108-110 “C. Xylene was refluxed over sodium and l’,l”-biphenylyl)]cyclotriphosphazene(5). A 250-mL, distilled, bp 137-144 “C. Aniline was refluxed over zinc dust heater-equipped, autoclave pressure bottle was charged with and distilled, bp 184-185 “C. Acetic anhydride was refluxed a solution of 2,2-bis(4’-nitrophenoxy)-4,4,6,6-bis[spiro(2’,2”over fused sodium acetate and distilled; bp 138-140 “C. dioxy-1’,1”-biphenylyl)lcyclotriphosphazene(4;12 g) in aniline Pyridine was refluxed over potassium hydroxide pellets and (90 mL). To this solution was added platinum oxide (0.04 g). distilled, bp 114-115 “C. Aromatic &anhydrides were purified The mixture was agitated at 40-50 “C and 40 psi of hydrogen by vacuum sublimation and tested before use on a differential for -2 h until no pressure drop was observed. Filtering off thermal analyzer (DTA). 3,3’,4,4’-Benzophenonetetracarboxy- the catalyst provided a clear solution, which was concentrated lic dianhydride (BTDA 7)and 4,4’-hexafluoroisopropylideneon a rotatory evaporator under reduced pressure. The residue diphthalic anhydride (6FDA 8 ) showed a single endotherm was treated with hexane. The product was filtered and dried a t 223 and 239-240 “C, respectively. to give a white solid (8 g, 75% yield). It was recrystallized from chlorobenzene and hexane to give a crystalline solid of Measurements. All NMR spectra were recorded on a 5; mp 304-306 “C. DSC: sharp endotherm a t 306.9 “C. Anal. Bruker WM-250 spectrometer with an Aspect 3000 computer. Calcd for C ~ G H ~ B N ~C, P ~60.1; O ~ :H, 3.9; N, 9.7; P, 12.9. The operating frequencies were 250.1 (‘HI and 101.2 MHz Found: C, 60.2; H, 4.0; N, 9.2; P, 13.0. IR (KBr pellet, cm-’1: (31P). Tetramethylsilane (Mersi) was used as an internal reference for ’H NMR measurements. For 31PNMR measurev 3470 and 3365 (N-H stretching of the amino group); 1619 ments 85% H3P04was used as an external standard. Chemiand 1592 (N-H bending, amino); 1508 and 1470 (aromatic); cal shifts downfield of the reference were assigned a posi1198, 1171 (P-N-P asymmetrical stretching of cyclotriphostive sign. 31PNMR spectra were recorded under conditions phazene); 780 (P-N-P symmetrical stretching of cyclotriphosphazene); 941 (P-N stretching of cyclotriphosphazene); of broad-band decoupling. Infrared spectra were recorded on a FT-Nicolet spectrophotometer on a KBr disk. Thermal 1258 (ether). IH-NMR (DMSO-d~):6 5.10 (s, 4H, =P(-Oanalysis was performed on a Perkin-Elmer thermal analysis C6&-”2)2, exchangeable to DzO), 6.64-6.67 (d, HA aroJ =9 matic, meta to amino groups {=P(-O-C~H~-NHZ)Z}, data station interfaced with a TGS-2 thermogravimetric Hz), 6.97-7.0 (dd, 4Hc aromatic, ortho to ether of dioxybiphesystem. D meta Synthesis. 2,2-Dichloro-4,4,6,6-bis[spiro(2’,2”-dioxy- nyl groups, J = 8 and 1.5 Hz), 7.17-7.2 (d, ~ H aromatic, to ether of dioxybiphenyl groups, J = 8 Hz), 7.43-7.55 (m, l’,l”-biphenylyl)]cyclotriphosphazene(3). To a three4H, and ~ H aromatic, F para and meta to ether of dioxybiphenyl necked, round-bottom flask equipped with a condenser and a ortho to amino groups groups), and 7.68-7.71 (d, ~ H aromatic, B guard tube, a nitrogen inlet, and a magnetic stirring bar, were J = 9 Hz). {=P(-O-C&4-NHz)z}, added chlorobenzene (50 mL), water (100 mL), hexachlorocy2,2-Bis(4-acetamidophenoxy)-4,4,6,6-bis[spiro(2,2-diclotriphosphazene (1; 6 g, 0.0172 mol), 2,2’-dihydroxy-l,l’(6). To a roundoxy-l’,l”-biphenylyl)]cyclotriphosphazene biphenyl (2;7 g, 0.038 mol), sodium hydroxide (2.2 g, 0.076 bottom flask equipped with a guard tube and a magnetic mol), and TBAB (0.56 g, 0.0018 mol). The reaction was rapidly stirring bar was added 2,2-bis(4‘-aminophenoxy)-4,4,6,6-bisstirred at room temperature for 3 h and then allowed to heat [spiro(2’,2”-dioxy-l’,1”-biphenylyl)lcyclotriphosphazene(5; 0.5 at 70 “C for another 3 h. The contents of the reaction mixture g) in acetic anhydride (5 mL). To this stirring mixture was was quenched with concentrated hydrochloric acid (14 mL). A added dry pyridine (0.1 mL). The clear solution was allowed white solid was obtained on flash evaporation of the reaction to stir overnight. The solution of the flask was poured over mixture. It was washed with a 5% aqueous potassium crushed ice to give a solid which was filtered and washed with hydroxide solution and then with water. The product was water. The obtained solid on drying gave a white compound recrystallized from acetone to give a shining crystalline solid (6)in 95% yield. Anal. Calcd for C40H32NbP308: C, 59.8; H, of 3 (7.9 g, 80% yield); mp 328-330 “C (lit.13 mp 325.7 “C). 4.0; N, 8.7; P, 11.6. Found: C, 60.0; H, 4.0; N, 8.8; P, 11.7. IR Mass spectrum, found mlz 573, calcd mlz 573. ‘H-NMR (KBr pellet, cm-I): v 1668 (carbonyl of CH3-CO-NH(CDC13): 6 7.26-7.56 (m, 16H, aromatic protons of two CsH40-); 1499 (aromatic); 1199, 1168 (P-N-P asymmetrical dioxybiphenyl groups). 2,2-Bis(4-nitrophenoxy~-4,4,6,6-bis[spiro(2,2”-dioxy- stretching of cyclotriphosphazene); 780 (P-N-P symmetrical stretching of cyclotriphosphazene); 935 (P-N stretching of l’,l”-biphenyly1)lcyclotriphosphazene(4). To a threecyclotriphosphazene); 1258 (ether). necked, round-bottom flask equipped with a nitrogen inlet and Polyimides Derived from BTDA,GFDA,and Diamine a Dean-Stark condenser with a guard tube was added 2,25 Containing Geminal Bis-Spiro-Substituted Cyclodichloro-4,4,6,6-bis[spir0-(2’,2”-dioxy-l’,1”-biphenylyl)lcyclotriphosphazene. The diamine, 2,2-bis(4’-aminophenoxy)triphosphazene (3)(30 g, 0.0523 mol) to dissolve in xylene (700 4,4,6,6-bis[spiro(2’,2’’-dioxy-l’,1”-biphenyly1)lcyclotriphosmL). To this stirring solution were added potassium 4-nitrophazene (5; 3.59 g, 0.005 mol) was dissolved in DMAC (29.52 phenoxide (19.1 g, 0.1078 mol) and TBAB (2 g). The reaction g, -17% solution w/w) in a dry flask equipped with a magnetic mixture was refluxed a t -130 “C with vigorous stirring and a

y)spiro-substituted cyclophosphazene-based diamine and polyimides therefrom.

Macromolecules, Vol. 28, No. 18, 1995

Aromatic Cyclolinear Phosphazene Polyimides 6325 Scheme 1

TBAB

+

g\

L

1

5

4

v

‘O 6

stirring bar. To this continuously stirred solution was added in one lot16 granular 3,3’,4,4’-benzophenonetetracarboxylic dianhydride (BTDA, 7;1.62 g, 0.005 mol), and the polymerization was performed at room temperature in a closed flask to give a viscous poly(amic acid) 9. A similar polymerization was carried out in rn-cresol. The inherent viscosity of the poly(amic acid) 9 in DMAC was 0.48 dug at a concentration of 0.5 g/dL at 30 “C. A N,N-dimethylacetamide(DMAC) solution (15-20% solids) of the poly(amicacid) 9 was spread on a clean, dry soda-lime glass plate with a doctor blade and dried to a tack-freefilm in a low-humidity chamber. The poly(amic acid) 9 film on thermal cyclodehydration 1h each at 100,200,and 300 “C in a forced oven in a nitrogen environment resulted in a lightyellow polyimide 11 film. The polyimide 12 was similarly synthesized by the condensation polymerization of the diamine 5 and 4,4’-hexafluoroisopropylidenediphthalic anhydride (6FDA; 8 ) in an equimolar quantity in DMAC, followed by thermal cyclodehydration of the resulting poly(amic acid) 10 at 160 “C for 0.5 h, 235 “C for 1.5 h, and 280 “C for 0.5 h. An almost colorless polyimide 12 film was obtained. The inherent viscosity of the poly(amic acid) 10 in DMAC was 0.50 dug at a concentration of 0.5 g/dL at 30 “C.

Results and Discussion The specific reaction sequences used for the synthesis of cyclotriphosphazene-containinglinear polyimides are given in Schemes 1 and 2. The diamine 2,2-bis(4’aminophenoxy)-4,4,6,6-bis [spiro(2’,2”-dioxy-1’,lf’-biphenylyl)]cyclotriphosphazene (5) has been synthesized for the first time. The cyclic trimer hexachlorocyclotriphosphazene (1) was conveniently reacted with 2,2’dihydroxy-l,lf-biphenyl(2) by a typical interfacial condensation reaction in the presence of a phase-transfer

catalyst (TBAB) using sodium hydroxide in water as an aqueous phase and chlorobenzene as an organic phase. A high-melting, soluble, white crystalline compound 2,2dichloro-4,4,6,6-bis[spiro(2’,2”-dioxy-lf,1”-biphenylyl)]cyclotriphosphazene (3) was obtained in pure form in high yield (-80%). No monosubstituted spiro product such as 2,2,4,4-tetrachloro-6,6-spiro(2’,2”-dioxy-l’,lffbiphenyly1)cyclotriphosphazene was isolated. This reaction provided a clean pathway to synthesize difunctional polymer-grade monomers required for the development of linear polymers. The dichloro compound 3 was characterized by lH-NMR, mass, and differential scanning calorimetry. The mass spectra showed M+ at mlz 573 consistent with its structure and indicated substitution at two phosphorus atoms by bis-spiro groups. The IR spectra showed bands assigned to the P-N stretching mode and biphenyl stretching mode. To examine the conformations assumed by the dioxybiphenyl unit, the X-ray crystal structure of 2,2,4,4tetrachloro-6,6-spiro(2’,2”-dioxyl’, 1”-biphenyly1)cyclotriphosphazene was obtained.17 The data demonstrated that the 0-P-0 bond angle was about 102.6”, similar to the reported18 C1-P-C1 bond angle of 101.8102”in hexachlorocyclotriphosphazene, indicating that the presence of a bulky seven-membered ring at phosphorus virtually has no effect in widening the 0-P-0 bond angle due to the marked twisting of the sevenmembered ring. The principal axis of the biphenyl group is twisted from the mean PN phosphazene ring plane. Furthermore, the average 41” twist between phenyl units within the biphenyl group further increases the molecular volume occupied by the substituents imparting thermal and chemical stability.

Macromolecules, Vol. 28, No. 18, 1995

6926 Kumar and Gupta

s +

pJRG0 t

Scheme 2 n

O

\

0

0

0

7 R= 8 R=

F3cxcF3

9

10

R=

R=

K

F3cxcF3

Table 1. slP NMR Spectral Data for Spiro(dioxybiphenyl)cyclotriphosphazenesa

*PZand 6 compound 4 6

6

PPm 30.54, 30.51 31.68, 31.65 31.40, 31.38

~ 3

HZ 29.61, 29.58,91.59 30.80, 30.77,88.20 30.47, 30.44, 89.00 Jppr

R NO2 NHz NHCOCH3

*P1 PPm 15.59, 14.69, 14.63, 13.73 17.33, 16.46, 16.43, 15.57 16.92, 16.04, 16.00, 15.12

Jpp, Hz 91.59 88.20 89.00

Pl:P2:P3 1:l:l 1:l:l 1:l:l

Structures given in Scheme 1.

The reaction of 2,2-dichloro-4,4,6,6-bis[spiro(2',2"dioxy-l',l"-biphenylyl)]cyclotriphosphazene(3)with potassium 4-nitrophenoxide in refluxing xylene provided the complete substitution. The water was removed as an azeotrope in the presence of a phase-transfer catalyst (TBAB). A white crystalline solid (4) in 90% yield was obtained. The differential scanning calorimetry of nitro compound 4 showed a sharp endotherm at 266 "C. The proton NMR of nitro compound 4 showed characteristic ortho-coupled doublets at 7.27-7.29 and 8.44-8.47 ppm, respectively, for eight aromatic protons of the two 4-nitrophenoxy groups. The downfield shift of the ortho protons to 8.44-8.77 ppm was characteri~ticl~ of the lnitrophenoxy group. The dioxybiphenyl aromatic protons were seen intact. The integration of the 4-nitrophenoxy aromatic protons to dioxybiphenyl aromatic protons was seen in a ratio of 1:2, confirming complete

sub-stitution of the intermediate dichlorocyclotriphosphazene derivative with 4-nitrophenoxy groups. The IR spectra showed characteristic bands for the presence of nitro groups, phosphazene, and bisspiro dioxybiphenyl ring. One of the most interesting features of compound 4 is connected with the overall conformations of the dioxybiphenyl side groups. The phosphorus-31 NMR spectra surprisingly did not show the expected A B 2 pattern. Further splitting was observed (Table 1).This indicated that the two phosphorus atoms attached to the dioxybiphenyl ring are not magnetically equivalent, and the molecule is not symmetrical. This nonequivalence of the two phosphorus atoms could be due to the difference in the angle of twist of the two phenyl groups of the biphenyl moieties and their twist in a different direction. The reason for this reversal twistfdistortion

Macromolecules, Vol. 28, No. 18, 1995

Aromatic Cyclolinear Phosphazene Polyimides 6327

could be due the advantageous thermodynamically, ’ - 49 stable seven-membereddioxybiphenyl ring conformation by imparting reduced 6,6‘ hydrogen-hydrogen contacts without broadening the 0-P-0 angle. The observation of a splitted doublet (Table 1)due to the two phosphorus atoms attached to the dioxybiphenyl groups indicates that such a conformationpossibly exists in the solution. This may be due to the fact that in solution either averaging of the conformational possibilities is not complete or the twisted biphenyls of the dioxybiphenyl sevenmembered spiro rings attend kinetically-stable confor. * . mations due to the intrinsic nature of the substitution groups. The nitro groups of 4 were catalytically reduced with molecular hydrogen in the presence of PtO2 to yield 2,2bis(4’-aminophenoxy)-4,4,6,6-bis [spiro(2’,2”-dioxy-l’,1”biphenylyl)lcyclotriphosphazene (5) in good yield. The 86 differential scanning calorimetery examination of the obtained diamine 5 showed a sharp endotherm at 306.9 CHEMICAL SHIFT,ppm “C. The crystalline, high-melting diamine 5 was soluble Figure 1. Plot of 31PNMR chemical shifi (6,) and coupling in THF, chlorobenzene, and aprotic solvents. An IR constant (J,,) values of bis(4-nitrophenoxy)bis[spiro(2‘,2”spectrum of 5 showed the absence of nitro stretching dioxy-1:”’- biphenylyl]cyclotriphosphazene(4) (01, bis(4-acwhich indicates the completion of reduction. Also, the etamidophenoxy)bis [spire(2’,2”-dioxy-l’,1”-biphenylyl)]cyclotriphosphazene (6)(+), and bis(4-nitrophenoxy)bis[spiro(2’,2”presence of amino, cyclotriphosphazene, and dioxybidioxy-l’,l”- biphenylyl)]cyclotriphosphazene (5) (0). phenyl groups was observed. Its proton NMR in deuterated DMSO showed the presence of two DzO exof the amino groups. The presence of phosphazene and changeable amino groups (four protons) along with eight dioxybiphenyl was seen intact. 31P-NMR spectra reortho-coupled aromatic protons of the two 4-aminophecorded in DMSO-& showed a splitted AB2 type of noxy groups and 16 aromatic protons of the two dioxypattern with a coupling constant of 89.0 Hz, indicating biphenyl groups; the 2:4:8 ratio of the respective protons the presence of two types of phosphorus in the cycloconfirmed the structure of diamine 5. The phosphorustriphosphazene ring due to acetamidophenoxyand spiro 31 NMR demonstrated two types of phosphorus atoms substituents (Table 1);however, the spiro-substituted in the cyclotriphosphazene ring due to aminophenoxy phosphorus atoms were seen magnetically nonequivaand spiro substituents (Table 1);however, the spirolent, similar to that observed in nitro compound 4 and substituted phosphorus atoms were seen magnetically amino compound 5. nonequivalent as found in nitro compound 4. On the The proton-decoupled 31PNMR spectral data obtained basis of the observed phosphorus-31 NMR magnetic for dioxybiphenyl-substituted spirocyclophosphazenes nonequivalance of the spiro-substituted phosphorus 4-6 are given in Table 1 and plotted in Figure 1. It atoms of the diamine 5 and the X-ray crystal structure of 2,2,4,4-tetrachloro-6,6-spiro(2’,2”-dioxy-1’,l”-biphe- was observed that the chemical shift positions of all three phosphorus atoms and their coupling constants nylyl)cyclotriphosphazene,17tris [spiro(2’,2”-dioxy-l’,1”are influenced by the presence of the nature of the biphenylyl)lcyclotriphosphazene,15 and 2,4-bis(4-aminophenoxy)-2,4-diphenoxy-6,6-diphenylcyclo- substitution [4-N02(4), 4-NH2 (51, or 4-NHCOCH3 (611 on the phenoxy group attached to one of the phosphorus triphosphazene,20it is believed the structure of diamine atoms (PI)of the cyclophosphazene ring. The net effect 5 may have twisted seven-membered spiro rings and of the respective substitution groups was such that the the side group conformations are arranged with phenyl P1 phosphorus resonance signals were observed most groups twisted in the opposite direction from the plane downfield for 4-aminophenoxygroup substituted phosof the cyclotriphosphazene ring. A perspective structure phorus and least for 4-nitrophenoxy group substituted of diamine 5 can be shown as phosphorus, and the order was 4-aminophenoxy > 4-acetamidophenoxy > 4-nitrophenoxy. A similar trend was observed for the chemical shift of the dioxybiphenylsubstituted phosphorus atoms (P2 and P3). However, a similar, but opposite, trend was observed for the coupling constants Hz). That is, the coupling constant was found lowest in the case of the 4-aminophenoxy group (88.2 Hz) and highest in the case of the 4-nitrophenoxy group (91.59 Hz), and the order was 4-nitrophenoxy > 4-acetamidophenoxy > 4-aminophenoxy. Also, a linear corelationship was found when the chemical shift values of the phosphorus atoms were plotted against the coupling constant values (Figure 1). It To further confirm the structure of diamine 5, its demonstrated that as the coupling constant increases acetylation was performed at room temperature with the chemical shift correspondingly decreases. acetic anhydride and pyridine. The obtained 2,2-bisCondensation polymerization of the diamine 5 with (4’-acetamidophenoxy)-4,4,6,6-bis[spiro(2‘,2“-dioxy-l’, 1“an equimolar amount of 3,3’,4,4‘-benzophenonetetrabiphenyly1)lcyclotriphosphazene (6) was characterized carboxylic dianhydride (BTDA; 7) was performed at by FT IR and 31P-NMR spectroscopy. The FT IR room temperature to give the corresponding poly(amic spectrum showed a band at 1668 cm-I due to the carbonyl of the acetamido group, indicating acetylation acid) 9. The polymerization was carried out by the two’

’

0

8

”

o

”

Macromolecules, Vol. 28, No. 18, 1995

6328 Kumar and Gupta .

. ._..__ .,,

. ..

--

_- ._

., ._

WAVENUMBERS

Figure 2. Infrared spectrum of polyimide 11 on a KBr disk.

I

I

I

I

I

I

"1 30

8

0

1

I

1

I

1

I

I

I

108

280

380

498

5E8

688

7E0

808

900

TEMPERATURE, "C

Figure 4. Thermogravimetric analysis of polyimides 11 and 12 in air. Conditions: gas flow rate, 100 mumin; heating rate, 20 "Clmin.

WAVENUMBERS

Figure 3. Infrared spectrum of polyimide 12 on a KBr disk.

stage polycondensation reaction. The first step of the condensation polymerization was performed in an aprotic solvent such as N,N-dimethylacetamide or in a phenolic solvent such as rn-cresol. The addition of a solid dianhydride was performed16 in one lot to avoid any premature hydrolysis of the dianhydride. The viscous solutions of the poly(amic acidls obtained can be stored for several days. Cyclodehydration, the second stage of imidization, of the tack-free film was carried out thermally 1 h each at 100, 200, and 300 "C in a forced oven in a nitrogen environment. The IR spectrum (Figure 2) of the obtained light-yellow polyimide 11 showed characteristic bands due to imide (1777 and 1718 cm-l), cyclophosphazene ring (1207, 1199, and 1167 cm-l), and aromatic groups. The band at 1670 cm-l was characteristic of the carbonyl of the benzophenone moiety. A colorless polyimide 12 film was similarly obtained by condensation polymerization of diamine 5 with 4,4'-hexafluoroisopropylidenediphthalic anhydride (6FDA 8 ) followed by cyclodehydration of the resulting poly(amic acid) 10 a t 160 "C for 0.5 h, 235 "C for 1.5 h, and 280 "C for 0.5 h . The infrared spectra (Figure 3) of this film showed characteristic imide (1784 and 1718 cm-l) bands. A cluster of bands due to CF3C-CF3 spread over 1253 cm-' from the 6FDA moiety were seen along with the phosphazene bands at 1198 and 1161 cm-l. The thermal stability of cyclotriphosphazene-containing aromatic polyimides 11 and 12 was investigated by dynamic thermogravimetry in air (Figure 4). The polyimides 11 and 12 showed thermooxidative decomposition starting at -410 "C and a char yield in the range of 58-50% at 800 "C in an air atmosphere. It

should be noted that such a high char yield is characteristic of these cyclotriphosphazene-containingpolyimides. Most of the available commercial linear polyimides degrade almost catastrophically in an air atmosphere beyond 600 "C without leaving any residue. In comparison to other phosphorus-containing linear polyimides,21the developed cyclotriphosphazene-containing polyimide films exhibit higher char yield at 800 "C in air. The observation of high char yield may be explained due to the presence of a higher percentage of phosphorus (in the form of a cyclotriphosphazene ring) per repeat unit of the polyimide chain in comparison to phosphorus-containing polyimides. Conclusion. We have developed a new class of cyclolinear polyimides containing bis(ary1enedioxy)spirocyclotriphosphazene as an integral part of the polymer chain and reported them here for the first time. In comparison to other polyimides that are now commercially available, these polyimides offer advantages of thermooxidative stability and high char yield in air. The possibility of regioisomeric mixture and contamination with tris- and terakisfunctional cyclophosphazenes has been conveniently removed in the diamine 5 by molecular design (selection of bis-spiro substituents) and proper synthetic procedures and pathway. The observation of high char yield in an air atmosphere, colorless to light-yellow color films, and bulky bis-spiro-substituted pendants makes cyclotriphosphazene-containing polyimides potential candidates for a variety of applications in space, aerospace, microelectronics, and membrane technologies.

Acknowledgment. The authors thank Prof. C. W. Allen of the Department of Chemistry, The University of Vermont, Burlington, VT, for providing a facility to record 31P-NMR and IH-NMR spectra. References and Notes (1) (a)Sroog, C. E. J.Polym. Sci., Macromol. Rev. 1976,11, 161 (b) Abadie, M.J. M.; Sillion, B., Eds. Polyimides and Other

High Temperature Polymers; Elsevier: Amsterdam, The Netherlands, 1991.

Macromolecules, Vol. 28, No. 18, 1995 (2)(a) Bessonov, M. I.; Koton, M. M.; Kudryavtsev, V. V.; Laius, L. A. Polyimides-Thermally Stable Polymers; Macromolecular Compounds Consultants Bureau: New York, 1987.(b) Feger, C., Khojasteh, M., McGrath, J. E., Eds. Polyimides, Materials, Chemistry and Characterization; Elsevier: Amsterdam, The Netherlands, 1989.(c). Stern, S. A.; Liu, y.; Feld, W. A. J. Polym. Sci., Part B: Polym. Phys. 1993,31, 939.Tanaka, K.; Kita, H.; Okano, M.; Okamoto, K. Polymer 1992,33(3), 585. Stathman, H. Membranes and Membrane Separation Processes. In Ullmann’s Encyclopedia of Industrial Chemistry, Elvers, B., Hawkins, S., Schultz, G., Eds.; VCH: Weinheim, 1990;Vol. A16, p 187. Cabasso, I. Membranes. In Encyclopedia of Polymer Science and Engineering; Mark, H. F., Bikales, N. M., Overberger, C. G., Menges, G., Eds.; John Wiley & Sons: New York, 1988;Vol. 9,p 509. (3)Kumar, D.;Fohlen, G. M.; Parker, J. A. Macromolecules 1983, 16,1250;U.S. Patent 4,634,759, 1987. (4) . . Allcock. H.R. PhosDhorus-Nitrogen - Compounds; Academic Press: New York, i972. (5) Kumar, D.:Fohlen, G. M.; Parker, J. A. J . Polym. Sci., Polym. Chem. Ed.’ 1983,21,2415. (6)Kumar, D.;Fohlen, G. M.; Parker, J. A. J. Polym. Sci.: Polym. Chem. Ed. 1984,22,927. (7)Kumar, D.;Fohlen, G. M.; Parker, J. A. J. Polym. Sci., Polym. Chem. Ed. 1984,22,1141. ( 8 ) Kumar, D. J. Polym. Sci., Polym. Chem. Ed. 1984,22,3439.

Aromatic Cyclolinear Phosphazene Polyimides 6329 (9)Kumar, D.;Khullar, M.; Gupta, A. D. Polymer 1993,34,3025. (10)Kumar, D.;Fohlen, G. M.; Parker, J. A. J. Polym. Sci., Polym. Chem. Ed. 1984,24,2415;US. Patent 4,668,589,1987. (11)Kumar, D.;Gupta, A. D.; Khullar, M. J. Polym. Sci., Part A: Polym. Chem. l993,31,707. (12)Banks, B. A.; Rutledge, S. K.; Paulsen, P. E.; Stueber, T. J. Simulation of Low Earth Orbital Atomic Oxygen Interaction with Materials by Means of an Oxygen Ion Beam. NASA TM101971;NASALewis Research Center, Cleveland, OH, 1989. (13)Pelc, R. A.; Brandt, K.; Jedlinski, Z. Phosphorus, Sulfur Silicon Relat. Elem. 1990,47;375. (14)Allcock, H.R.; Siegal, L. A. J. Am. Chem. SOC.1964,86,5140. (15)Allcock, H. R.; Stein, M. T.; Stanko, J. A. J. Am. Chem. SOC. 1971,93(131,3173 . (16)Kumar, D.;Gupta, A. D. Polym. Adu. Technol. 1992,3,1. (17)Kumar, D.;Gupta, A. D. Unpublished work. (18)Wilson, A.; Carroll, D. F. J. Chem. SOC.1960,2548. (19)Kumar, D.;Gupta, A. D.; Khullar, M. J. Polym. Sci.; Part A: Polym. Chem. 1993,31,2739. (20)Kumar, D.;Allen, C. W. Unpublished work. (21)Martinez-Nuiiez, M. F.; Sekhripuram, V. N.; McGrath, J. E. Polym. Prepr. (Am. Chem.SOC.,Diu. Polym. Chem.) 1994,35 (21,710.Lin, Y. N.;Joardar, S.; McGrath, J. E. Polym. Prepr. (Am. Chem. SOC.,Diu. Polym. Chem.) 1993,34(11,515.

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